Department of Pathology, UNESP - Univ Estadual Paulista, 18618-970, Botucatu-São Paulo, Brasil.
Mutagenesis. 2011 May;26(3):415-20. doi: 10.1093/mutage/geq109. Epub 2011 Jan 21.
There are numerous studies reporting on the effects of inhalation anaesthesia in cells of exposed individuals but not much is known about the ability of isoflurane (ISF) to induce oxidative DNA damage. However, surgery is often associated with a temporary perioperative immunological alteration, and some volatile anaesthetics seem to contribute to a transient lymphocytopenia after surgery. We conducted a study to evaluate a possible genotoxic effect, including oxidative DNA damage, and apoptosis in peripheral lymphocytes of 20 patients American Society of Anaesthesiologists physical status I undergoing minor elective surgery lasting at least 120 min, under anaesthesia with ISF. We also investigated the expression of several genes in blood cells. Blood samples were collected at three time points: before anaesthesia (T(1)), 2 h after the beginning of anaesthesia (T(2)) and on the first post-operative day (T(3)). General DNA damage and oxidised bases (Fpg and endo III-sites) in blood lymphocytes were evaluated using the comet assay. Lymphocytes were phenotyped and apoptosis was evaluated by flow cytometry. In addition, expressions of hOGG1 and XRCC1, genes involved in DNA repair, and BCL2, a gene related to apoptosis, were assessed by quantitative real-time polymerase chain reaction. Results showed no statistically significant difference in the level of DNA damage and oxidised bases among the three sampling times. Anaesthesia with ISF did not increase the percentage of cells in early or late apoptosis in cytotoxic or helper T lymphocytes. Lower hOGG1 and BCL2 expressions were detected at T(3) in comparison to the other two previous time points, and there was significantly lower expression of XRCC1 at T(3) in relation to T(2). In conclusion, the exposure to ISF did not result in genotoxicity and cytotoxicity in lymphocytes and in toxicogenomic effect in leukocytes, although DNA repair and apoptosis-related genes were down-regulated on the first post-operative day.
有许多研究报告了吸入麻醉在暴露个体细胞中的作用,但对于异氟醚(ISF)诱导氧化 DNA 损伤的能力知之甚少。然而,手术通常与围手术期的短暂免疫改变有关,一些挥发性麻醉剂似乎会导致手术后短暂的淋巴细胞减少。我们进行了一项研究,以评估接受小选择性手术的 20 名美国麻醉医师协会身体状况 I 级患者的外周淋巴细胞中可能存在的遗传毒性效应,包括氧化 DNA 损伤和细胞凋亡,这些患者在异氟醚麻醉下至少持续 120 分钟。我们还研究了血细胞中几个基因的表达。在三个时间点采集血样:麻醉前(T(1))、麻醉开始后 2 小时(T(2))和术后第一天(T(3))。使用彗星试验评估血液淋巴细胞中的总 DNA 损伤和氧化碱基(Fpg 和内切酶 III 位点)。通过流式细胞术对淋巴细胞进行表型分析并评估凋亡。此外,通过定量实时聚合酶链反应评估与 DNA 修复相关的 hOGG1 和 XRCC1 基因以及与凋亡相关的 BCL2 基因的表达。结果显示,在三个采样时间点之间,DNA 损伤和氧化碱基的水平没有统计学差异。异氟醚麻醉并未增加细胞毒性或辅助性 T 淋巴细胞中早期或晚期凋亡细胞的百分比。与前两个时间点相比,T(3)时 hOGG1 和 BCL2 的表达降低,与 T(2)相比,T(3)时 XRCC1 的表达显著降低。总之,异氟醚暴露并未导致淋巴细胞的遗传毒性和细胞毒性,也未导致白细胞的毒性基因组效应,尽管在术后第一天,与 DNA 修复和凋亡相关的基因表达下调。